89794-15-0 Usage
Description
2-Amino-6-(bromomethyl)-4(3H)-pteridinone is a brown solid that serves as a key reactant in the synthesis of bisubstrate analog inhibitors targeting hydroxymethyl dihydropterin pyrophosphokinase. 2-AMino-6-(broMoMethyl)-4(3H)-pteridinone plays a significant role in the development of pharmaceuticals and biochemistry research.
Uses
Used in Pharmaceutical Industry:
2-Amino-6-(bromomethyl)-4(3H)-pteridinone is used as a reactant for the preparation of bisubstrate analog inhibitors of hydroxymethyl dihydropterin pyrophosphokinase. These inhibitors are crucial in the development of drugs that can modulate the activity of this enzyme, which is implicated in various metabolic pathways and diseases.
Used in Biochemistry Research:
In the field of biochemistry, 2-Amino-6-(bromomethyl)-4(3H)-pteridinone is utilized as a building block for the synthesis of novel compounds with potential biological activities. Its unique structure allows researchers to explore its interactions with various biomolecules and enzymes, contributing to a better understanding of biological processes and the discovery of new therapeutic agents.
Synthesis Reference(s)
Journal of Heterocyclic Chemistry, 24, p. 279, 1987 DOI: 10.1002/jhet.5570240154
Check Digit Verification of cas no
The CAS Registry Mumber 89794-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,9 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89794-15:
(7*8)+(6*9)+(5*7)+(4*9)+(3*4)+(2*1)+(1*5)=200
200 % 10 = 0
So 89794-15-0 is a valid CAS Registry Number.
89794-15-0Relevant articles and documents
Folic acid synthesis method
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Paragraph 0033; 0034, (2016/12/26)
The present invention relates to a folic acid synthesis method. According to the present invention, with the method, a 2,4,5-triamino-6-hydroxypyrimidine salt, 3-halogenated pyruvaldehyde oxime and N-(4-aminobenzamide)-L-glutamic acid are subjected to a reaction to prepare the folic acid; and the 3-halogenated pyruvaldehyde oxime is used to replace the low purity 1,1,3-trichloroacetone, such that the generation of a large amount of waste water in the traditional method is avoided, the reaction conditions are mild, the operation is easy, the reaction selectivity is good, the product purity is high, the advantages of safety and environmental protection are provided, and the method is suitable for the industrial requirements on environmental protection.
